EDLAW PHARMACEUTICALS, INC.

FDA Device Registration & Listing · E Farmingdale, NY, US · Registration 2431908

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2431908
FEI Number
2431908
Entity Name
EDLAW PHARMACEUTICALS, INC.
City/State/Country
E Farmingdale, NY, US
Establishment Address
195-B CENTRAL AVE., E Farmingdale, NY 11735, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
EDLAW PHARMACEUTICALS, INC. (Owner Number: 2431908)
Owner / Operator Contact Address
195-B CENTRAL AVE., --, Farmingdale, NY 11735, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Hemo-Dial

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder) Gastroenterology, Urology Class 2 876.5820 2016-02-16

Official Correspondent

BONNIE HILTON GREEN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EDLAW PHARMACEUTICALS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2431908. Last updated year: 2026. Please use registration number 2431908 when referencing this establishment in official correspondence.
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